A composition useful as a paint remover, including alkylene carbonate such as propylene carbonate or ethylene carbonate, and an alcohol such as benzyl alcohol. Also, a process for removing paint, comprising: applying a composition containing alkylene carbonate and an alcohol to a painted surface for a time and under conditions effective to reduce adhesion between the top coats and the primer or undercoat of the paint. In another aspect, this paint remover includes dialkyl carbonate and an alcohol, optionally containing a glycol ether. In another aspect, the process includes applying a composition containing dialkyl carbonate and an alcohol. This paint remover may include a thickener, a surfactant, or a corrosion inhibitor.

Patent
   6548464
Priority
Nov 28 2000
Filed
Nov 28 2000
Issued
Apr 15 2003
Expiry
Nov 28 2020
Assg.orig
Entity
Large
7
51
EXPIRED
1. A process for removing paint, comprising: applying a composition comprising from 92 to 99 weight percent of an alkylene carbonate and from 1 to 8 weight percent of an alcohol.
7. A process for removing a coating from a surface, comprising:
providing a miscible composition of from 92 to 99 weight percent of alkylene carbonate and from 1 to 8 weight percent of an alcohol;
adding a thickening agent to the miscible composition, and mixing the resulting composition to form a thickened composition;
applying the thickened composition to a coated surface having two or more layers of coating for a time sufficient and under conditions effective to separate at least one layer of coating from the remaining layers; and
removing the separated coating layer and thickened composition from the surface.
2. The process recited in claim 1, wherein the alcohol is benzyl alcohol.
3. The process recited in claim 1, wherein the alkylene carbonate is propylene carbonate.
4. The process recited in claim 1, wherein the composition further comprises a surfactant.
5. The process recited in claim 1, wherein the composition further comprises an organic solvent.
6. The process recited in claim wherein the composition further comprises an corrosion inhibitor.
8. The process recited in claim 7, wherein the coating is paint.
9. The process recited in claim 7, wherein the alkylene carbonate is propylene carbonate.
10. The process recited in claim 9, wherein the thickened composition contains about 90 to about 99.5 percent by weight propylene carbonate, and about 0.1 to about 10 percent by weight alcohol, wherein the alcohol further comprises benzyl alcohol.
11. The process recited in claim 7, wherein the surface is aluminum.

This invention relates to compositions for paint and coating removal. More particularly, this invention relates to compositions containing an alkylene carbonate or dialkyl carbonate or both, and an alcohol.

Paint removing compositions are commonly used in industry, such as for stripping paint from airplane fuselages. Conventional paint remover compositions include methylene chloride, phenol, or caustic. Each of these materials, however, has inherent problems during use. While methylene chloride based compositions are very effective as paint removers, methylene chloride is a highly volatile material that is considered toxic. Phenol is also highly toxic. Caustic, while not posing problems with toxicity, can burn and corrode aluminum. Additionally, methylene chloride, phenol or caustic-based strippers will attack, soften and remove all layers of paint including the primer or undercoat, making selective removal difficult.

In some applications it is desirable to be able to remove one or more layers of coating, while leaving the priming coats intact. Aircraft applications are examples of situations in which it is not desirable to remove all of the paint layers. By removing the upper coating layers while leaving the highly toxic chromium-based primer material intact, the paint removal process would generate much less hazardous waste and thus be much less costly to perform. Due to the deficiencies and disadvantages of conventional paint removing compositions, new paint removing compositions, especially those capable of selective removal, are highly desirable.

The invention is a composition useful as a paint remover, comprising alkylene carbonate and an alcohol. This composition may also contain a thickener, a surfactant, or a corrosion inhibitor.

In another broad aspect, this invention is a process for removing paint, comprising applying a composition containing alkylene carbonate and an alcohol to a painted surface for a time, and under conditions effective to cause separation of the interface between the topcoats and the primer or undercoat of the paint. The composition may also contain a thickener, a surfactant, or a corrosion inhibitor.

In another broad aspect, this invention is a process for removing paint, comprising applying a composition containing an alkylene carbonate, a dialkyl carbonate, or both and an alcohol to a painted surface for a time, and under conditions effective to reduce adhesion between the topcoats and the primer or undercoat of the paint. The composition may also contain a thickener, a surfactant, or a corrosion inhibitor.

In another broad aspect, this invention is a process for removing paint, comprising applying a composition containing a dialkyl carbonate and an alcohol to a painted surface for a time, and under conditions effective to reduce adhesion between the topcoats and the primer or undercoat of the paint. The composition may also contain a thickener.

The surfaces to be treated may be sealed with a variety of sealants, such as polysulfide, polyurethane, lacquer, epoxy, and the like. The compositions can be used to remove paints and coatings from furniture, automobiles, boats, trains, airplanes, military vehicles, and so forth.

The present invention has a number of advantages. For example, the compositions have several important attributes, including low toxicity, high efficacy in removing paint and coatings, and neutral pH (or slightly acidic or slightly basic pH). Furthermore, in the case of propylene carbonate, the propylene carbonate breaks down into propylene glycol, which is non-toxic. Thus, the propylene carbonate compositions of this invention are environmentally friendly, particularly as compared to chlorinated hydrocarbons and the like which are commonly used for paint and coating removal. In addition, the compositions of this invention reduce adhesion between the topcoats and the primer or undercoat of the paint in such a short period of time that it is envisioned that the compositions of this invention might be applied in liquid form, as opposed to the gels that are commonly used.

The compositions of the present invention have surprisingly superior paint removing properties. The compositions may be blended with additional co-solvents, corrosion inhibitors, surfactants and thickeners, or may be used directly to effect paint removal. The compositions of this invention are nonflammable, of low volatility, and free of carcinogenic chemicals.

The compositions of this invention contain an alkylene carbonate or a dialkyl carbonate or both, and an alcohol.

The alkylene carbonate used in the present invention can contain from 3 to 10 carbon atoms. Representative examples of alkylene carbonates that may be employed in the practice of this invention include, but are not limited to, ethylene carbonate, propylene carbonate and butylene carbonate, but the preferred carbonate is propylene.

The dialkyl carbonate used in the present invention may contain from 3 to 25 carbon atoms. The dialkyl carbonate may be of formula R--CO3--R', wherein R and R' may be the same or different, and may independently in each occurrence be an alkyl group of from 1 to about 12 carbon atoms. In one embodiment, the dialkyl carbonate may be dimethyl carbonate, diethyl carbonate, or a mixture of those two.

The compositions of this invention include an alcohol. Representative examples of such alcohols include methanol, ethanol, propanol, butanol, and benzyl alcohol, but the preferred alcohol is benzyl. Generally, compositions of this invention contain from about 0.1 to about 10 percent by weight alcohol.

In certain embodiments of this invention, the compositions contain from about 90 to about 99.9 percent by weight alkylene carbonate. In certain other embodiments of this invention, the compositions contain from about 90 to about 99.9 percent by weight dialkyl carbonate, and from about 0.01 to 10 percent alcohol.

In addition to the components described above, the compositions of this invention may optionally contain thickeners, glycol ethers such as propylene glycol methyl ether (PM), dipropylene glycol methyl ether (DPM), or dipropylene glycol n-butyl ether (DPNB), surfactants, stabilizers, corrosion inhibitors, and other additives commonly used in paint removers.

Thickeners may be used in the present invention include, but are not limited to, cellulose ethers such hydroxypropyl cellulose, ethyl cellulose, ethyl hydroxyethyl cellulose, methyl cellulose, and other alkyl or hydroxyalkyl cellulose, silica including colloidal silica, clays such as bentonite and montmorillonite starch, alumina including colloidal alumina, high molecular weight polyethylene oxides, polyvinyl pyrrolidone and methyl vinyl ether/maleic anhydride copolymers. Certain hydroxy alkyl cellulose ethers and certain experimental polymers are particularly effective and resistant to breakdown in the practice of this invention. Such cellulose ethers are available commercially from The Dow Chemical Company under the trade name Methocel® F4MPRG and Dow's Experimental Polymer SCS 41067.06. When a thickener is used, the amount of such thickener can vary depending on the desired level of thickening for the given application. In general, the amount of thickener employed is about 1 to about 4 percent by weight.

Corrosion inhibitors that may be used in the present invention include, but are not limited to, ethoxylated butynediol, petroleum sulfonates, blends of propargyl alcohol and thiourea. If used, the amount of such corrosion inhibitors is typically up to about 10% by weight of the total composition.

Surfactants which may optionally be used in the practice of this invention include, but are not limited to, non-ionic, anionic, cationic and amphoteric surfactants, such as monocarboxyl cocoimidoazoline, higher alkyl sulfate sodium salts, tridecyloxy poly(alkyleneoxy ethanol), ethoxylated or propoxylated alkyl phenol, alkyl sulfoamides, C10-18 alkylaryl sulfonates such as alkylbenzene sulfonates, cocoamphaodipropionate, hydrogenated castor oil, isooctylphenyl polyethoxy ethanol, sorbitan monopahnitate, C8-18 alkyl pyrrolidone, and cocoaminopropionic acid. When used, the amount of surfactant should be sufficient to render the composition miscible. In the context of this invention, the term "miscible solution" or "miscible composition" means a single phase solution. Typically the amount of surfactant is from about 0.1 to about 10 percent by weight of the total composition.

The compositions of the present invention may contain a wide variety of other organic co-solvents. Likewise, the present invention may be practiced in the absence of one or more of such solvents. Non-limiting examples of representative classes of such co-solvents include hydrocarbons, glycols, glycol ethers, glycol ether esters, ethers, esters, phenols, glycols, sulfur-based solvents, chlorinated hydrocarbons, aromatic hydrocarbons nitrated hydrocarbons, amides, and ketones. Such co-solvents may be polar or non-polar, may be protic or aprotic, may be cyclic, branched, or straight chain, and may contain one or more functional groups. Representative examples of common hydrocarbon solvents include hexane, toluene, xylene, and mixtures of aliphatic and aromatic hydrocarbons.

Examples of common ether co-solvents that may be used in the present invention include, but are not limited to, dibutyl ether, ethyl ether, and diphenyl ether. Representative examples of common phenols include, but are not limited to, phenol and the Cresols and resorcinols. Representative examples of common glycol solvents include, but are not limited to, ethylene, propylene and butylene glycols as well as methyl propane diol.

Examples of common sulfur-based co-solvents that can be used in the present invention include, but are not limited to, dimethylsulfoxide (DMSO) and sulfolane. Representative examples of common chlorinated hydrocarbon co-solvents include, but are not limited to, methylene chloride, methyl chloroform, chlorobenzenes and dichlorobenzenes. Representative examples of common nitrated hydrocarbon co-solvents include, but are not limited to, nitroethane and nitropropane. Representative examples of common amide co-solvents include, but are not limited to, formamide, dimethyl formamide, acetamide, and dimethylacetamide. Representative examples of common ketone co-solvents include, but are not limited to, acetone, methyl ethyl ketone (MEK), and methyl isobutyl ketone and methyl isoamylketone.

When a given composition containing dialkyl carbonate does not form a miscible composition, a co-solvent may be used to provide a miscible composition. For instance, a glycol ether may be added as a co-solvent in an amount effective to dissolve the components of the mixture. Such glycol ethers may be included for other purposes as well. Such amounts may vary depending on the specific composition of interest, as one of skill in the art may appreciate. Also, an alcohol or alkylene carbonate may be beneficially employed as a co-solvent to provide miscible dialkyl carbonate compositions of this invention.

A practitioner may use the paint stripping process of this invention under a variety of conditions. Typically, one may conduct the process under ambient atmospheric conditions, although both elevated and decreased temperatures can be used. One may apply the paint remover composition by any convenient method such as dipping, spraying, or brushing the composition onto the paint surface. For resistant painted surfaces it may be desirable to apply the composition two or more times to fully separate the topcoats from the primer or undercoat of the paint. It may be desirable to use a rag, scraper, abrasive blaster, or the like to fully remove the loosened paint from the primer or undercoat after the paint remover composition has been given time to fully act. Alternatively, high-pressure water spray may be employed to remove paint and residual paint remover composition. The time required for the paint remover composition to act will vary due to a variety of factors such as temperature, paint type, paint thickness and the particular paint remover formulation being used. In general, application times are between one minute and one hour, although longer application times may be used.

The following examples are illustrative of this invention and are not intended to limit the scope of the claimed subject matter of the present invention. Unless otherwise denoted all percentages are by weight.

Various compositions were prepared containing propylene carbonate, as indicated in Table 1. In Table 1, BA represents benzyl alcohol and PC represents propylene carbonate. The times listed in Table 1 refer to the contact times of the compositions with the painted surface before the pencil test was performed.

TABLE I
FORMULATIONS AND PENCIL
HARDNESS TEST DATA
Formulations Time
BA (%) PC (%) 30 min 1 hr 1.5 hr 2 hr 2.5 hr
Topcoat
8 92 H* H* H* 3B 3B
5 95 H* H* H* 3B 3B
3 97 H H H* 3B 3B
2 98 H H H* H H
1 99 H H H* H H
Primer Coat
8 92 3B 3B 3B 3B 3B
5 95 H H H H H
3 97 H H H H H
2 98 H H H H H
1 99 3B 3B 3B 3B 3B
*indicates that the topcoat separated from the intact primer coat

The compositions were applied to a standard aluminum panel having paint and coatings for military use (obtained from Scientific Material International, Inc. of Miami, Fla., Lot 96046-A2 4"×5", MIL-P-2337 primer, MIL-S-81733 Type 3 polysulfide sealant, MIL-C-83286), and allowed to sit on the panels. The propylene carbonate/benzyl alcohol compositions were surprisingly effective in reducing the adhesion between the topcoat and the primer coat.

The Pencil Hardness data indicates the ease of separation of the topcoat from the primer or undercoat. The indicated hardness, e.g. H or 3B, is the softest pencil lead that scored the surface of the topcoat under the stated conditions.

The compositions have several important attributes, including low toxicity, high efficacy in removing paint and coatings, and neutral pH (or slightly acidic or slightly basic pH). Furthermore, propylene carbonate breaks down into propylene glycol, which is nontoxic. Thus, the propylene carbonate compositions of this invention are environmentally friendly, particularly as compared to chlorinated hydrocarbons and the like which are commonly used for paint and coating removing. In addition, the compositions of this invention cause breakdown of the interface between the topcoat and the primer or undercoat in such a short period of time that the compositions of this invention can be applied in liquid form, as opposed to the gels that are commonly applied. However, on difficult to remove coatings on vertical surfaces, thickeners such as Klucel H (Hercules, Aqualon Division), Dow's Methocell® F4MPRG, or Dow's experimental polymer XCS 41067.06 may be required to obtain effective coating removal.

Marquis, Edward T., Machac, Jr., James R., Woodrum, Susan A., Nieh, Edward Chung-Yit

Patent Priority Assignee Title
11054749, May 22 2018 VERSUM MATERIALS US, LLC Photoresist stripping composition and method
7304021, Nov 17 2005 Dynacraft Industries, Inc Color changing paint and varnish remover
8198226, Nov 17 2005 Sunnyside Corporation Color changing paint and varnish remover
8361947, Apr 30 2007 Peel Away Limited Paint remover
8383565, Nov 17 2005 Dynacraft Industries, Inc Color changing paint and varnish remover
8603258, Sep 14 2004 Church & Dwight Co., Inc. Paint and ink remover two-phase system
9987212, Jun 04 2015 L Oreal Acetone-deficient composition
Patent Priority Assignee Title
3285777,
3355385,
3843578,
3925008,
3954648, Dec 22 1969 ATOCHEM NORTH AMERICA, INC , A PA CORP Coatings removal composition containing an alkali metal hydroxide, an oxygenated organic solvent, and an amine
4508634, Nov 15 1983 Minnesota Mining and Manufacturing Company; MINNESOTA MINING AND MANUFACTURING COMPANY ST PAUL MN A DE CORP Aqueous skin cleaner composition comprising propylene carbonate
4561898, Sep 30 1983 Henkel Kommanditgesellschaft auf Aktien Hardener for silicate soil stabilizers
4594111, Oct 04 1984 PHILADELPHIA CHEMCIAL COMPANY, THE; COONAN, ANNA D Liquid phase cleaner-solvent
4780235, Apr 16 1987 E. I. du Pont de Nemours and Company Paint remover
4927556, Jun 04 1987 Minnesota Mining and Manufacturing Company Aqueous based composition containing dibasic ester and thickening agent for removing coatings
4956115, May 23 1989 Hoechst Celanese Corporation Water borne solvent strippers
5006279, Aug 24 1988 Henkel Corporation Water-based coating removers
5007969, May 20 1988 The Boeing Company; Boeing Company, the Low toxicity liquid solvent
5049300, Oct 01 1990 VERONA INC A DE CORP Method of activating acidified NMP to provide an effective paint remover composition
5064557, Oct 15 1990 ISP CAPITAL, INC Resin cleaner composition
5084200, Aug 07 1989 PETROFERM INC , A DE CORP Cleaning composition of dibasic ester, hydrocarbon solvent, compatibilizing surfactant and water
5085795, Feb 21 1991 ISP 3 CORP; ISP Investments Inc Water-based compositions for removing stains from fabrics
5098591, Jun 30 1989 Stevens Sciences Corp. Paint stripper and varnish remover compositions containing organoclay rheological additives, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
5098594, May 20 1988 The Boeing Company; Boeing Company, the Carbonate/diester based solvent
5106525, Apr 12 1991 Arco Chemical Technology, Inc Paint stripper compositions containing gamma-butyrolactone
5124062, Jun 30 1989 Stevens Sciences Corp. Paint stripper and varnish remover compositions, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
5178788, Nov 08 1990 HUNTSMAN PETROCHEMCIAL CORPORATION Co-solvent system for removing cured fiberglass resin and cured flexible or rigid urethane foams from substrates
5179224, Apr 11 1986 Mitsui Toatsu Chemicals, Incorporated Preparation process of cinnamate ester
5183514, Apr 01 1991 HUNTSMAN PETROCHEMCIAL CORPORATION Process for dissolving or removing rigid polyurethane foam by contacting with 1,2-dimethyl imidazole
5204026, May 20 1988 The Boeing Company Solvent with alicyclic carbonate and ethylene dipropionate
5215675, Mar 16 1992 ISP CAPITAL, INC Aqueous stripping composition containing peroxide and water soluble ester
5236614, Sep 25 1990 Colgate-Palmolive Company Stable microemulsion disinfecting detergent composition
5298081, Nov 19 1990 HUNTSMAN PETROCHEMCIAL CORPORATION Process for removing cured fiberglass resin from substrates
5331103, Feb 26 1992 Rhone-Poulenc Chimie Process for monohydroxylation of phenolic compounds
5334331, Jan 12 1993 ISP Investments Inc. Method of activating N-methyl-2-pyrrolidone (NMP) varnish and paint remover solvents for removal of organic coatings
5346640, Aug 30 1989 Transcontinental Marketing Group, Inc.; TRANSCONTINENTAL MARKETING GROUP, INC , THE Cleaner compositions for removing graffiti from surfaces
5414153, Apr 03 1992 Rhone-Poulenc Chimie Hydroxylation of phenolic compounds
5425893, Apr 14 1993 Photoreactive paint stripping compositions and methods
5427710, Apr 14 1993 Paint stripping compositions and methods
5449474, Feb 21 1992 Inland Technology, Inc. Low toxicity solvent composition
5518661, Oct 15 1993 Minnesota Mining and Manufacturing Company Paint stripper containing benzyl alcohol or alkyl-substituted derivative and methylene chloride or other chlorinated alkane
5585526, Jan 08 1993 Rhone-Poulenc Chimie Preparation of P-fuchsones and synthesis of P-Dihydroxylated aromatic compounds therefrom
5597788, Apr 14 1993 Paint stripping compositions and methods
5665690, Feb 21 1992 Inland Technology Incorporated Low toxicity solvent composition
5721204, Feb 29 1996 Gage Products Company Paint stripping composition
5728666, Dec 19 1996 FREEWORLD COATINGS GLOBAL PTY LTD Water-based alcohol hydroxycarboxylic peroxide compositions and their preparation
5741368, Jan 30 1996 Silicon Valley Chemlabs; SILICON VALLEY CHEMLABS, INC Dibasic ester stripping composition
6040284, May 23 1997 JPMORGAN CHASE BANK, N A , AS COLLATERAL AGENT Paint coatings remover comprising propylene carbonate and hydrogen peroxide
6130192, Aug 04 1999 FREEWORLD COATINGS GLOBAL PTY LTD Paint stripper and cleaning compositions
EP507426,
EP845525,
WO63304,
WO9103522,
WO9318102,
WO9729158,
WO9853016,
/////////////////
Executed onAssignorAssigneeConveyanceFrameReelDoc
Nov 28 2000Huntsman Petrochemical Corporation(assignment on the face of the patent)
Feb 07 2001MARQUIS, EDWARD T Huntsman Petrochemical CorporationASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0115990108 pdf
Feb 07 2001WOODRUM, SUSAN A Huntsman Petrochemical CorporationASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0115990108 pdf
Feb 07 2001NIEH, EDWARD CHUNG-YITHuntsman Petrochemical CorporationASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0115990108 pdf
Feb 07 2001MACHAC, JAMES R , JR Huntsman Petrochemical CorporationASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0115990108 pdf
Sep 30 2002Huntsman Petrochemical CorporationDEUTSCHE BANK TRUST COMPANY AMERICAS FORMERLY KNOWN AS BANKERS TRUST COMPANY , AS AGENTSECURITY INTEREST SEE DOCUMENT FOR DETAILS 0133620237 pdf
Sep 30 2003Huntsman Petrochemical CorporationDEUTSCHE BANK TRUST COMPANY AMERICAS FORMERLY KNOWN AS BANKER TRUST COMPANY , AS COLLATERAL AGENTGRANT OF SECURITY INTEREST IN U S TRADEMARKS AND PATENTS 0147820186 pdf
Oct 14 2004HUNSTMAN PETROCHEMICAL CORPORATIONDEUTSCHE BANK TRUST COMPANY AMERICAS, AS AGENTSECURITY AGREEMENT0156610547 pdf
Aug 16 2005Huntsman Petrochemical CorporationDEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AGENTSECURITY INTEREST SEE DOCUMENT FOR DETAILS 0169870496 pdf
Feb 02 2011DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT F K A BANKERS TRUST COMPANY, AS COLLATERAL AGENT Huntsman Petrochemical LLCRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0257650853 pdf
Feb 02 2011DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT F K A BANKERS TRUST COMPANY, AS COLLATERAL AGENT HUNTSMAN ETHYLEMEAMINES LLCRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0257650853 pdf
Feb 02 2011DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT F K A BANKERS TRUST COMPANY, AS COLLATERAL AGENT Huntsman Advanced Materials Americas LLCRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0257650853 pdf
Feb 02 2011DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT F K A BANKERS TRUST COMPANY, AS COLLATERAL AGENT Huntsman Advanced Materials LLCRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0257650853 pdf
Feb 02 2011DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT F K A BANKERS TRUST COMPANY, AS COLLATERAL AGENT Huntsman International LLCRELEASE BY SECURED PARTY SEE DOCUMENT FOR DETAILS 0257650853 pdf
Feb 23 2011DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENTJPMORGAN CHASE BANK, N A , AS COLLATERAL AGENTASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS 0258570137 pdf
Feb 23 2011DEUTSCHE BANK TRUST AG NEW YORK BRANCH, AS RESIGNING ADMINISTRATIVE AGENT AND COLLATERAL AGENTJPMORGAN CHASE BANK, N A , AS COLLATERAL AGENTCORRECTIVE ASSIGNMENT TO CORRECT THE NATURE OF CONVEYANCE FROM AN ASSIGNMENT TO A SECURITY AGREEMENT PREVIOUSLY RECORDED ON REEL 025857 FRAME 0137 ASSIGNOR S HEREBY CONFIRMS THE ASSIGNMENT 0265150641 pdf
May 21 2018JPMORGAN CHASE BANK, N A HUNTSMAN PETROCHEMICAL CORPORATION N K A HUNTSMAN PETROCHEMICAL LLC TERMINATION AND RELEASE OF SECURITY INTEREST IN UNITED STATES TRADEMARKS AND PATENTS0463560616 pdf
Date Maintenance Fee Events
Oct 12 2006M1551: Payment of Maintenance Fee, 4th Year, Large Entity.
Nov 22 2010REM: Maintenance Fee Reminder Mailed.
Apr 15 2011EXP: Patent Expired for Failure to Pay Maintenance Fees.


Date Maintenance Schedule
Apr 15 20064 years fee payment window open
Oct 15 20066 months grace period start (w surcharge)
Apr 15 2007patent expiry (for year 4)
Apr 15 20092 years to revive unintentionally abandoned end. (for year 4)
Apr 15 20108 years fee payment window open
Oct 15 20106 months grace period start (w surcharge)
Apr 15 2011patent expiry (for year 8)
Apr 15 20132 years to revive unintentionally abandoned end. (for year 8)
Apr 15 201412 years fee payment window open
Oct 15 20146 months grace period start (w surcharge)
Apr 15 2015patent expiry (for year 12)
Apr 15 20172 years to revive unintentionally abandoned end. (for year 12)